[go: up one dir, main page]

WO2008018520A1 - Procédé de préparation dérivé d'acide hydroxycarboxylique optiquement actif ou de son sel - Google Patents

Procédé de préparation dérivé d'acide hydroxycarboxylique optiquement actif ou de son sel Download PDF

Info

Publication number
WO2008018520A1
WO2008018520A1 PCT/JP2007/065559 JP2007065559W WO2008018520A1 WO 2008018520 A1 WO2008018520 A1 WO 2008018520A1 JP 2007065559 W JP2007065559 W JP 2007065559W WO 2008018520 A1 WO2008018520 A1 WO 2008018520A1
Authority
WO
WIPO (PCT)
Prior art keywords
group
hydrogen
optically active
reaction
carbon atoms
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2007/065559
Other languages
English (en)
Japanese (ja)
Inventor
Susumu Amano
Akio Fujii
Shohei Yamamoto
Masaru Mitsuda
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kaneka Corp
Original Assignee
Kaneka Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kaneka Corp filed Critical Kaneka Corp
Priority to JP2008528863A priority Critical patent/JPWO2008018520A1/ja
Priority to US12/376,803 priority patent/US8058471B2/en
Priority to EP07805906A priority patent/EP2053032A4/fr
Publication of WO2008018520A1 publication Critical patent/WO2008018520A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B53/00—Asymmetric syntheses
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • C07C201/06—Preparation of nitro compounds
    • C07C201/12—Preparation of nitro compounds by reactions not involving the formation of nitro groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/367—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of functional groups containing oxygen only in singly bound form
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07—Optical isomers

Definitions

  • the present invention relates to a method for producing an optically active hydroxycarboxylic acid derivative that can be used for general purposes.
  • Optically active hydroxycarboxylic acid derivatives are important intermediates in the production of pharmaceuticals, agricultural chemicals and chemical products.
  • ketocarboxylic acid derivative represented by the formula (wherein R 1 is an optionally substituted alkyl group having 1 to 20 carbon atoms, Y represents hydrogen or metal), or a salt thereof is General formula (3):
  • Non-Patent Document 2 a method using an optically active reducing agent
  • Patent Document 2 a method using an optically active ligand
  • Patent Document 1 WO2005 / 049816
  • Patent Document 2 US4614806
  • Non-Patent Document 1 Tetrahedron: Asymmetry, 2004, 15 (23), 3763.
  • Non-Patent Document 2 Tetrahedron Letters, 1998, 39, 5501.
  • Non-Patent Document 3 Chiralyty, 1991, 3 (4), 370.
  • the present invention is intended to efficiently produce optically active hydroxycarboxylic acid derivatives important in the production of pharmaceutical products and the like from various ketocarboxylic acid derivatives or salts thereof. is there.
  • the present invention provides a ketocarboxylic acid derivative represented by the above formula (1) or a salt thereof.
  • R 2 and R 3 represent an optionally substituted alkyl group having 1 to 20 carbon atoms and an optionally substituted aryl group having 6 to 14 carbon atoms.
  • R 4 represents Represents an optionally substituted alkyl group having 1 to 20 carbon atoms and an optionally substituted aryl group having 6 to 14 carbon atoms
  • R 5 represents an optionally substituted alkyl group having 1 to 20 carbon atoms
  • An aryl group having 6 to 14 carbon atoms which may be substituted and hydrogen
  • Ar represents an aromatic compound which may be substituted
  • M represents a transition metal
  • X represents a halogen atom
  • * represents no An optically active diamine complex represented by the formula (3) and a hydrogen transfer-type reduction reaction in the presence of a hydrogen-donating compound.
  • the present invention relates to a method for producing an active hydroxycarboxylic acid derivative or a salt thereof.
  • the reduction reaction is performed by a hydrogen transfer type reduction reaction.
  • the hydrogen transfer reduction reaction is a reaction in which a reaction substrate is reduced by transferring a hydrogen atom from a hydrogen donating compound to the reaction substrate.
  • a hydrogen donating compound an easily handleable compound such as an acid or an alcohol is used, and a dangerous hydrogen gas or a metal hydride reagent that is not easily handled, which is generally used in a reduction reaction, is not used.
  • the reaction is possible under mild conditions and no special equipment is required.
  • the optically active diamine complex represented by the above formula (2) is used in the reduction reaction.
  • the optically active diamine complex of the above formula (2) is stable to moisture, oxygen, etc. unlike ordinary transition metal catalysts, and it is not easy to handle because it does not require strict moisture and oxygen removal during the reaction. is there. Moreover, it can be synthesized at low cost because it can be synthesized from general-purpose diamine.
  • the alkyl group having 1 to 20 carbon atoms of ⁇ to may be, for example, a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, Tinole group, sec butyl group, tert butyl group, n pentyl group, isopentyl group, n hexyl group, n octyl group, cyclopentyl group, cyclohexyl group, hydroxymethyl group, chloromethylol group, benzinole group, o, m, p Nitrobenzinole group, p-chlorobenzene group, 4 methylbenzyl group, 3 methylbenzyl group, 2 methylbenzyl group, 4-methoxybenzyl group, 3 methoxybenzyl group, 2 methoxybenzyl group, 1 phenylethyl group, 2 1 Examples
  • substituents include, but are not limited to, a force S including an alkyl group, aryl group, amino group, nitro group, sulfonyl group, halogen atom, hydroxyl group, alkoxyl group, and the like.
  • the aryl group having 2 to 14 carbon atoms of R 2 to R 5 which may be substituted includes, for example, a phenyl group, a p hydroxyphenyl group, a 1 naphthyl group, a 2 naphthyl group, a 4 methylphenyl group, 3 Methylphenyl group, 2 Methylphenyl group, 4 Ethylphenyl group, 3 Ethynolephenyl group, 4-Methoxyphenyl group, 3 Methoxyphenyl group, 2 Methoxyphenyl group, 4-12 Trophenylenole group, 4 Phenylenophenyl group, 4 The ability to list a phenylol group, 4-bromophenyl group, etc.
  • substituent include the same substituents as described above, but are not limited thereto.
  • the carbon number represents a number not including the carbon number of the substituent.
  • the production method of the present invention has the general formula (1):
  • a hydrogen transfer reduction reaction is performed in the presence of an optically active diamine complex represented by the formula:
  • the method comprises preparing an optically active hydroxycarboxylic acid derivative represented by:
  • R 1 represents an optionally substituted alkyl group having 1 to 20 carbon atoms.
  • R 1 is preferably a methyl group, an ethyl group, an isopropyl group, a tert-butyl group, an n-octyl group, a hydroxymethyl group, a chloromethyl group, a benzyl group, o-, m- or p-nitro.
  • a force S that can include a benzyl group, a 2-phenylethyl group, and the like, but is not limited thereto.
  • a methyl group, an ethyl group, an isopropyl group, a tert-butyl group, an n-octyl group, a hydroxymethyl group, a chloromethyl group, a benzyl group, an o-, m- or p-nitrobenzyl group, or a 2-phenylethyl group is there.
  • Y represents hydrogen or a metal atom.
  • the metal atom include alkali metals such as lithium, sodium and potassium, alkaline earth metals such as magnesium and calcium, halogenated earth metals such as magnesium chloride and calcium chloride, and aluminum. Power It is not limited to these.
  • Y is preferably hydrogen, alkali metal, alkaline earth metal or halogenated earth metal, and more preferably hydrogen.
  • the ketocarboxylic acid derivative in which Y is hydrogen is an amine and a salt. It can be used in the same manner in the form of a ketocarboxylate salt formed.
  • amines include, but are not limited to, ammonia, methylamine, ethylamine, phenylethylamine, diisopropylamine, triethylamine, aniline, lutidine, and the like.
  • R 2 and R 3 represent an optionally substituted alkyl group having 1 to 20 carbon atoms and an optionally substituted aryl group having 6 to 14 carbon atoms.
  • R 2 and R 3 may be the same or different, and may be joined together to form a ring.
  • R 2 and R 3 are preferably a methyl group, an ethyl group, an isopropyl group, a tert butyl group, an n octyl group, a hydroxymethyl group, a chloromethyl group, a phenyl group, a p-hydroxyphenyl group, a benzyl group, o-, m Forces that can include — or p-tolyl group, o-, m- or p-anisyl group, p-chlorobenzyl group, naphthyl group, tetramethylene group and the like are not limited to these. More preferably, R 2 and R 3 are both a phenyl group, or R 2 and R 3 are a tetramethylene group formed together to form a ring.
  • R 4 represents an optionally substituted alkyl group having 1 to 20 carbon atoms and an optionally substituted aryl group having 6 to 14 carbon atoms.
  • R 4 is preferably a methyl group, an ethyl group, an isopropyl group, a tert butyl group, an n-octyl group, a hydroxymethyl group, a chloromethyl group, a trifluoromethyl group, a benzyl group, a phenylol group, or a p-hydroxy group.
  • Phenyl group o-, m or p nitrophenyl group, o-, m- or p-trinole group, o-, m- or p-trifluoromethylphenyl group, p-chlorobenzene group, 2 , 4, 6 Trimethylenophenyl group, 2, 4, 6 Triisopropinorephenylol group, 6 Trimethoxyphenyl group, Naphtyl group, 2, 4, 6 Triclonal phenyl group, etc. It is not limited to these.
  • R 4 is a methyl group, a trifluoromethylol group, a phenylol group, p ⁇ !; A no group, a p ⁇ !; A funole age romethino lepheninole group, or a 2, 4, 6 HJ chlorophenyl group. Particularly preferred is a p-tolyl group.
  • R 5 represents an optionally substituted alkyl group having 1 to 20 carbon atoms, an optionally substituted aryl group having 6 to 14 carbon atoms, or hydrogen.
  • R 5 is preferably hydrogen, methyl group, ethyl group, isopropyl group, tert butyl group, n-octyl group, hydroxymethyl group, chloromethyl group, phenyl group, p-hydroxyphenyl group, benzyl group. Group, p-chlorobenzoyl group, naphthyl group and the like are not limited thereto. More preferably, R 5 is hydrogen or a methyl group. Particularly preferred is hydrogen.
  • Ar represents an optionally substituted aromatic compound. Specifically, benzene, toluene, xylene, mesitylene, hexamethylbenzene, ethyl benzene, tert-butynolebenzene, p-cymene, tamen, pentamethinorecyclopentadiene, etc. It is not limited to. Ar is preferably p-cymene, benzene, mesitylene, or pentamethylcyclopentadenyl. More preferred is p-cymene.
  • M represents a transition metal.
  • power that can include palladium, rhodium, ruthenium, iridium, platinum, zirconium, titanium, chromium, cobalt, copper, nickel, zinc, manganese, iron, ytterbium, lanthanum, etc. It is not something. Ruthenium, rhodium and iridium are preferred. More preferably, ruthenium.
  • X represents a halogen atom.
  • Specific examples include fluorine, chlorine, nitrogen and iodine. Preferably it is chlorine.
  • * represents an asymmetric carbon.
  • the configuration of the asymmetric carbon atom may be either) or (S).
  • R 2 and R 3 are both a phenyl group or a tetramethylene group in which R 2 and R 3 are joined together to form a ring, both are (R) or both are (S) I prefer to be! /
  • * similarly represents an asymmetric carbon.
  • the configuration of the asymmetric carbon atom may be either (R) or (S).
  • the amount of the optically active diamine complex represented by the formula (2) used in the hydrogen transfer type reduction reaction step is not particularly limited, but the ketocarboxylic acid represented by the formula (1), In addition, it is usually equivalent to 0.00001 to; equivalent (preferably (0.001 to 0.1 equivalent, more preferably 0.0001 to 0.01 equivalent).
  • the hydrogen donating compound used is not particularly limited, but alcohol, formic acid or a formic acid salt is preferred.
  • alcohol formic acid or a formic acid salt
  • Specific examples of the alcohol include, but are not limited to, methanol, ethanol, n-propanol, isopropanol and the like. Isopropanol is preferred.
  • Examples of the formic acid salt include, but are not limited to, sodium formate and ammonium formate.
  • the hydrogen-donating compound is preferably formic acid or isopropanol, and more preferably formic acid.
  • a base coexists.
  • the base include organic amines and inorganic bases.
  • the inorganic base include, but are not limited to, sodium hydroxide, potassium hydroxide, potassium carbonate, and the like.
  • organic amines include, but are not limited to, a force S including trimethylamine, triethylamine, ammonia, and the like.
  • the combination of a hydrogen donating compound and a base is most preferably a combination of formic acid and triethylamine.
  • the amount of the hydrogen-donating compound used is not particularly limited.
  • formic acid it is usually 1 to 100 equivalents with respect to the compound represented by the formula (1). !! to 10 equivalents, more preferably 1 to 3 equivalents.
  • the amount of ammine used is not particularly limited.
  • triethylamine is generally 0.0;! To 100 with respect to the compound represented by the formula (1).
  • Equivalents preferably 0.;! To 10 equivalents, more preferably 1 to 4 equivalents.
  • a reaction solvent is not particularly required, and it is preferable to carry out the reaction without a solvent because the reaction can be completed in a very short time and the equivalent amount of catalyst can be reduced.
  • a reaction solvent may be used, in which case there is no particular limitation on the reaction solvent species.
  • the reaction solvent used for the reaction is water, an organic solvent, or a mixed solvent of water and an organic solvent.
  • the organic solvent is not particularly limited, and examples thereof include alcohol solvents such as methanol, ethanol, butanol, isopropanol, ethylene glycol, and methoxy alcohol; carbonization such as benzene, toluene, n hexane, and cyclohexane.
  • alcohol solvents such as methanol, ethanol, butanol, isopropanol, ethylene glycol, and methoxy alcohol
  • carbonization such as benzene, toluene, n hexane, and cyclohexane.
  • Hydrogen solvents such as jetyl ether, tetrahydrofuran, 1,4 dioxane, methyl t butyl ether, dimethoxyethane, ethylene glycol dimethyl ether; ethyl acetate, acetic acid Ester solvents such as butyl; Ketone solvents such as acetone and methyl ethyl ketone; Halogen solvents such as methyl chloride, chloroform, 1,1,1-trichloroethane; Acetonitrile, acetamide, dimethylformamide, etc.
  • ether solvents such as jetyl ether, tetrahydrofuran, 1,4 dioxane, methyl t butyl ether, dimethoxyethane, ethylene glycol dimethyl ether; ethyl acetate, acetic acid Ester solvents such as butyl; Ketone solvents such as acetone and methyl ethyl ketone; Halogen solvents such as
  • Nitrogen-containing solvents such as dimethyl sulfoxide, dimethylacetamide, N-methylpyrrolidone, hexamethylphosphoric triamide and the like. These may be used alone or in combination of two or more.
  • solvent-free, alcohol-based solvent, hydrocarbon-based solvent, ether-based solvent, ester-based solvent, ketone-based solvent, rhodium-based, solvent-based solvent, and aprotic polar solvent When no solvent or alcohol solvent is used, the optical purity of the reaction product is particularly high. Particularly preferred is solventless or methanol.
  • the concentration in the case of using a reaction solvent is not particularly limited, but the concentration of the compound represented by the formula (1) with respect to the solvent is preferably 40% or less, more preferably 30% or less, Particularly preferably 20% or less.
  • the lower limit is not particularly limited, but is preferably 5% or more.
  • a lower concentration is preferable, but in the case of a non-solvent, surprisingly, the compound represented by the formula (3) is highly stereoselectively contrary to the above. can get.
  • the reaction temperature is preferably 40 ° C to 160 ° C, more preferably 20 ° C to 100 ° C. Particularly preferred is 0 to 60 ° C.
  • the reaction procedure in this step is not particularly limited, and the order of addition of the compounds represented by the formulas (1) and (2) and the hydrogen-donating compound is not particularly limited, but the formulas (1) and ( It is preferable to add a hydrogen donating compound to the mixture of 2).
  • the hydrogen-donating compound and the base may be mixed and added to the mixture of the formulas (1) and (2), but the mixture of the formulas (1) and (2) may be added. It is preferable to add the hydrogen-donating compound after adding the base.
  • the hydrogen-donating compound may be added and reacted at once, or may be reacted while adding continuously or intermittently. From the viewpoint of safety, it is preferable to add the strength sequentially as the reaction proceeds.
  • the addition time is not particularly limited, but it is preferable to add the gas generated as the reaction proceeds at a rate at which it can be safely exhausted.
  • the time required to add the whole amount is preferable Is 30 minutes or more, particularly preferably 1 hour or more.
  • optically active diamine complex represented by the formula (2) may be prepared in advance, isolated and purified, or prepared in a system and used.
  • the obtained reaction solution may be subjected to the next step, but in order to obtain a product from the reaction solution, a general post-treatment may be performed.
  • a general post-treatment may be performed after completion of the reaction.
  • the pH of the reaction solution is adjusted as necessary, and an extraction operation is performed using a general extraction solvent such as ethyl acetate, jetyl ether, methylene chloride, toluene, hexane and the like.
  • the target product is obtained by distilling off the reaction solvent and the extraction solvent from the obtained extract by an operation such as heating under reduced pressure.
  • the reaction solvent may be distilled off by an operation such as heating under reduced pressure, and then the same operation may be performed. Good.
  • the target product obtained in this manner may be purified by a general method such as force S, crystallization purification, fractional distillation, column chromatography, etc., which is almost pure, and the purity may be further increased.
  • the obtained object may be dried using a dryer or the like.
  • the solvent used for crystallization varies depending on the compound and is not particularly limited.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

L'invention concerne un procédé de préparation d'un dérivé d'acide hydroxycarboxylique optiquement actif qui est un intermédiaire important pour la préparation de produits pharmaceutiques, de produits chimiques agricoles, de produits chimiques et analogues. Ce procédé de préparation est caractérisé en ce qu'un dérivé d'acide hydroxycarboxylique optiquement actif est préparé en faisant agir un complexe diamine optiquement actif sur un acide cétocarboxylique, ou un sel de celui-ci, pour entraîner une réaction de réduction par transfert d'hydrogène. Par ce procédé, un dérivé d'acide hydroxycarboxylique optiquement actif commercialement avantageux peut être préparé de manière sûre et efficace.
PCT/JP2007/065559 2006-08-09 2007-08-08 Procédé de préparation dérivé d'acide hydroxycarboxylique optiquement actif ou de son sel Ceased WO2008018520A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2008528863A JPWO2008018520A1 (ja) 2006-08-09 2007-08-08 光学活性ヒドロキシカルボン酸誘導体又はその塩の製造法
US12/376,803 US8058471B2 (en) 2006-08-09 2007-08-08 Method for producing optically active hydroxycarboxylic acid derivatives or salts thereof
EP07805906A EP2053032A4 (fr) 2006-08-09 2007-08-08 Procédé de préparation dérivé d'acide hydroxycarboxylique optiquement actif ou de son sel

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2006-216771 2006-08-09
JP2006216771 2006-08-09

Publications (1)

Publication Number Publication Date
WO2008018520A1 true WO2008018520A1 (fr) 2008-02-14

Family

ID=39033050

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2007/065559 Ceased WO2008018520A1 (fr) 2006-08-09 2007-08-08 Procédé de préparation dérivé d'acide hydroxycarboxylique optiquement actif ou de son sel

Country Status (4)

Country Link
US (1) US8058471B2 (fr)
EP (1) EP2053032A4 (fr)
JP (1) JPWO2008018520A1 (fr)
WO (1) WO2008018520A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010248091A (ja) * 2009-04-10 2010-11-04 Kanto Chem Co Inc 不斉触媒およびこれを用いた光学活性アルコール類の製造方法

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4614806A (en) 1983-12-23 1986-09-30 American Home Products Corporation Process for the asymmetric synthesis of chiral indoline-2-carboxylic acids
JPS63316744A (ja) * 1987-06-19 1988-12-26 Takasago Corp 光学活性アルコ−ルの製造方法
JPH07502410A (ja) * 1991-12-23 1995-03-16 ジェンザイム・リミテッド ホモキラル性の２−ヒドロキシ酸の合成
JPH09157196A (ja) * 1995-12-06 1997-06-17 Kagaku Gijutsu Shinko Jigyodan 光学活性アルコール類の製造方法
JPH10120621A (ja) * 1996-10-24 1998-05-12 Takeda Chem Ind Ltd 光学活性化合物の製造法
JP2000053593A (ja) * 1998-06-19 2000-02-22 Degussa Huels Ag エステル化合物および酸化合物の均一触媒によるエナンチオ選択的な水素添加のための方法および水素添加生成物の使用
JP2001199928A (ja) * 2000-01-24 2001-07-24 Mitsubishi Chemicals Corp 光学活性α−ヒドロキシケトン類の製造方法
JP2003034665A (ja) * 2001-05-18 2003-02-07 Takasago Internatl Corp 光学活性アルコールの製造方法
WO2005049816A2 (fr) 2003-11-21 2005-06-02 Juelich Enzyme Products Gmbh Oxydoreductase de metschnikowia zobellii

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0967015B1 (fr) 1998-06-19 2005-01-12 Degussa AG Utilisation de ligands ferrocenyl pour l'hydrogénation catalytique énantioselective

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4614806A (en) 1983-12-23 1986-09-30 American Home Products Corporation Process for the asymmetric synthesis of chiral indoline-2-carboxylic acids
JPS63316744A (ja) * 1987-06-19 1988-12-26 Takasago Corp 光学活性アルコ−ルの製造方法
JPH07502410A (ja) * 1991-12-23 1995-03-16 ジェンザイム・リミテッド ホモキラル性の２−ヒドロキシ酸の合成
JPH09157196A (ja) * 1995-12-06 1997-06-17 Kagaku Gijutsu Shinko Jigyodan 光学活性アルコール類の製造方法
JPH10120621A (ja) * 1996-10-24 1998-05-12 Takeda Chem Ind Ltd 光学活性化合物の製造法
JP2000053593A (ja) * 1998-06-19 2000-02-22 Degussa Huels Ag エステル化合物および酸化合物の均一触媒によるエナンチオ選択的な水素添加のための方法および水素添加生成物の使用
JP2001199928A (ja) * 2000-01-24 2001-07-24 Mitsubishi Chemicals Corp 光学活性α−ヒドロキシケトン類の製造方法
JP2003034665A (ja) * 2001-05-18 2003-02-07 Takasago Internatl Corp 光学活性アルコールの製造方法
WO2005049816A2 (fr) 2003-11-21 2005-06-02 Juelich Enzyme Products Gmbh Oxydoreductase de metschnikowia zobellii

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
CHIRALITY, vol. 3, no. 4, 1991, pages 370
See also references of EP2053032A4
TETRAHEDRON LETTERS, vol. 39, 1998, pages 5501
TETRAHEDRON: ASYMMETRY, vol. 15, no. 23, 2004, pages 3763

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010248091A (ja) * 2009-04-10 2010-11-04 Kanto Chem Co Inc 不斉触媒およびこれを用いた光学活性アルコール類の製造方法

Also Published As

Publication number Publication date
EP2053032A1 (fr) 2009-04-29
US8058471B2 (en) 2011-11-15
US20100191011A1 (en) 2010-07-29
EP2053032A4 (fr) 2012-04-04
JPWO2008018520A1 (ja) 2010-01-07

Similar Documents

Publication Publication Date Title
EP2817289B1 (fr) Procédés de synthèse asymétrique pour la préparation de composés d'aminosulfone
JP6574474B2 (ja) キラルジペプチジルペプチダーゼ−ｉｖ阻害剤の製造方法
AU2004236085A1 (en) Processes for producing 3-substituted 2-chloro-5-fluoropyridine or salt thereof
FR2840303A1 (fr) Procede d'arylation ou de vinylation ou d'alcylynation d'un compose nucleophile
EP1509502A1 (fr) Procede de formation d une liaison carbone-carbone ou carbone-heteroatome
Carmona et al. Asymmetric organocatalytic synthesis of tertiary azomethyl alcohols: Key intermediates towards azoxy compounds and α-hydroxy-β-amino esters
JP5843186B2 (ja) ピロール及びインドール誘導体とその製造方法
WO2008018520A1 (fr) Procédé de préparation dérivé d'acide hydroxycarboxylique optiquement actif ou de son sel
EP2197829A2 (fr) Procede de synthese d'arylamines
CN101977899A (zh) 哌啶-3-基氨基甲酸酯化合物的制造方法及其光学拆分方法
AU2021308138A1 (en) Method for producing optically active compound
JP3902384B2 (ja) 光学活性α−メチル−ビス−３，５−（トリフルオロメチル）ベンジルアミン類の精製方法
Dhara et al. An iron-catalyzed domino reaction of donor–acceptor cyclopropanes: a diastereoselective approach towards diversely functionalized pyrrolo-quinazolines
JP2022075375A (ja) 光学活性アミン化合物の製造方法
EP1907377B1 (fr) Procede de preparation d'almotriptane
CN111018807A (zh) 一种合成1,2,4-噻二唑衍生物的方法
CN115504921A (zh) 一种C(sp3)-H官能化引发的1,5-烯腈制备吡咯烷-2,4-二酮衍生物方法
JP2002363160A (ja) 光学活性４−アリール−２−ピペリジノン類の製造方法
JP2004300036A (ja) β−アラニン誘導体およびその製造方法
WO2001019779A1 (fr) Preparation d'amines primaires halogenees
JP2004115439A (ja) Ｌ−フェニレフリンの製造方法
JP6255343B2 (ja) Ｄ−アロイソロイシンの製造方法
CN102958889A (zh) 用于制备α-酮羧酸的方法
WO2002006187A1 (fr) Procede de preparation d'un compose polyaromatique
WO2010045352A2 (fr) Procédés de production d’acides aminonitrobenzoïques

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 07805906

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2008528863

Country of ref document: JP

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2007805906

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: RU

WWE Wipo information: entry into national phase

Ref document number: 12376803

Country of ref document: US